7074-59-1 Usage
Molecular weight
256.27 g/mol
Structure
Purine derivative with a benzyl group attached to the nitrogen atom at position 1 and a carbonyl group at position 6
Biological activities
a. Inhibits adenosine deaminase enzyme
b. Blocks conversion of adenosine to inosine
c. Increases adenosine levels in the body
Potential therapeutic applications
a. Treatment of cancer
b. Treatment of neurological disorders
Mechanism of action
a. Modulates adenosine receptors
b. Exhibits anti-inflammatory effects
Appearance
Likely a solid or crystalline compound (based on molecular weight and structure)
Solubility
Soluble in organic solvents (e.g., methanol, ethanol, dimethyl sulfoxide) and possibly water to some extent
Stability
Stable under normal conditions, but sensitive to heat, light, and moisture
Reactivity
May react with strong acids, strong bases, and nucleophiles due to the presence of carbonyl and aromatic groups
Synthesis
Typically synthesized through chemical reactions involving purine derivatives and benzyl groups
Safety and handling
Handle with care, using appropriate personal protective equipment (PPE) such as gloves, goggles, and lab coats. Avoid inhalation, ingestion, and skin contact. Store in a cool, dry, and dark place, away from heat and light sources.
Check Digit Verification of cas no
The CAS Registry Mumber 7074-59-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,7 and 4 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7074-59:
(6*7)+(5*0)+(4*7)+(3*4)+(2*5)+(1*9)=101
101 % 10 = 1
So 7074-59-1 is a valid CAS Registry Number.
7074-59-1Relevant articles and documents
Synthesis of 2′,3′-dideoxyinosine via radical deoxygenation
Torii, Takayoshi,Izawa, Kunisuke,Cho, Dae Hyan,Jang, Doo Ok
, p. 985 - 988 (2008/03/28)
A synthetic method for 2′,3′-dideoxyinosine (ddI) from inosine was established via radical deoxygenation of N1,5′-O-diprotected-2′, 3′-bis-S-methyl dithiocarbonate of inosine derivatives. The radical deoxygenation proceeded smoothly to give the desired dideoxy compounds in good yields using 1-ethylpiperidinium hypophosphite and triethylborane. Benzyl or p-methoxybenzyl protection of inosine at the N1, 5′-O-positions were effective for the ddI synthesis. Copyright Taylor & Francis Group, LLC.
